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rs876658575

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658575(C;T)
Make rs876658575(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68828302
GeneCDH1
is asnp
is mentioned by
dbSNPrs876658575
ebirs876658575
HLIrs876658575
Exacrs876658575
Varsomers876658575
Maprs876658575
PheGenIrs876658575
hapmaprs876658575
1000 genomesrs876658575
hgdprs876658575
ensemblrs876658575
gopubmedrs876658575
geneviewrs876658575
scholarrs876658575
googlers876658575
pharmgkbrs876658575
gwascentralrs876658575
openSNPrs876658575
23andMers876658575
23andMe allrs876658575
SNP Nexus

SNPshotrs876658575
SNPdbers876658575
MSV3drs876658575
GWAS Ctlgrs876658575
Max Magnitude0
ClinVar
Risk rs876658575(T;T)
Alt rs876658575(T;T)
Reference rs876658575(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene CDH1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000016.9:g.68862205C>T
CLNSRC
CLNACC RCV000222740.1,